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HP-β-CD

HP-β-CD
HP-β-CD (HP-β-CD) is a widely used drug delivery vehicle to improve stability and bioavailability.
Catalog No. T19609Cas No. 128446-35-5
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HP-β-CD

Catalog No. T19609Alias Hydroxypropyl-β-cyclodextrin, Hydroxypropyl betadexCas No. 128446-35-5

HP-β-CD (HP-β-CD) is a widely used drug delivery vehicle to improve stability and bioavailability.
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Pack SizePriceAvailabilityQuantity
500 mg$33In Stock
1 g$48In Stock
5 g$68In Stock
10 g$89In Stock
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Product Introduction

Bioactivity
Description
HP-β-CD (HP-β-CD) is a widely used drug delivery vehicle to improve stability and bioavailability.
In vitro
Cell treatment with (2-hydroxypropyl)-β-cyclodextrin can activate the activation of the transcription factor EB (the main regulator of lysosomal function and autophagy) and enhance the cell's autophagy clearance ability[1]. HP-β-CD treatment reduces intracellular cholesterol resulting in significant leukemic cell growth inhibition through G2/M cell-cycle arrest and apoptosis. The IC50 values for HP-β-CD after 72 hours exposure are in the range of 3.86–10.09 mM. HP-β-CD also shows anticancer effects against CML cells expressing a T315I BCR-ABL mutation (that confers resistance to most ABL tyrosine kinase inhibitors), and hypoxia-adapted CML cells that have characteristics of leukemic stem cells. In addition, colony forming ability of human primary AML and CML cells is inhibited by HP-β-CD[2].
In vivo
Intraperitoneal injection of HP-β-CD significantly improves survival in leukemia mouse models. Systemic administration of HP-β-CD to mice has no significant adverse effects[2].
AliasHydroxypropyl-β-cyclodextrin, Hydroxypropyl betadex
Chemical Properties
Molecular Weight1541.5
FormulaC63H112O42
Cas No.128446-35-5
Storage & Solubility Information
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 45 mg/mL (29.19 mM)
H2O: 50 mg/mL, Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM0.6487 mL3.2436 mL6.4872 mL32.4359 mL
5 mM0.1297 mL0.6487 mL1.2974 mL6.4872 mL
10 mM0.0649 mL0.3244 mL0.6487 mL3.2436 mL
20 mM0.0324 mL0.1622 mL0.3244 mL1.6218 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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